Colonoscopy surveillance in Lynch syndrome is burdensome and frequently delayed.

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Familial Cancer Pub Date : 2023-10-01 Epub Date: 2023-05-12 DOI:10.1007/s10689-023-00333-4
Elsa L S A van Liere, Imke L Jacobs, Evelien Dekker, Maarten A J M Jacobs, Nanne K H de Boer, Dewkoemar Ramsoekh
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Abstract

Individuals with Lynch syndrome have an increased colorectal cancer risk, hence, biennial colonoscopy surveillance is recommended. We aimed to investigate patients' perception and preferences regarding surveillance, and to further explore compliance behaviour. Individuals with Lynch syndrome received a validated survey evaluating experiences of their three most recent colonoscopies. Individuals were non-compliant to surveillance if the interval between colonoscopies differed ≥ 6 months from the recommended interval. In total, 197 of 291 (68%) invited individuals returned the survey. They mostly underwent colonoscopy biennially (99%), under mild sedation (79%) and with bowel preparation performed by Moviprep® (99%). Surveillance was perceived as impacting quality of life in 21%, and as moderately to extremely burdensome in 57%, particularly in those below age 40. To lower the burden, patients prioritised improvements in volume and taste of bowel preparation, laxation-related bowel movements, waiting times, and a more personal and respectful approach of endoscopic staff. Additionally, many individuals (60%) would favour less-invasive surveillance modalities such as biomarkers. In total, 28% of individuals had delayed colonoscopy surveillance, predominantly for patient-related reasons. An additional 10% considered quitting/postponing surveillance. Upon multivariable analysis, patient-related delay was associated with low and medium education, history of ≤ 4 colonoscopies and having no hospital recall-system. Colonoscopy surveillance in Lynch syndrome is often experienced as burdensome, and frequently delayed. We identified determinants of surveillance behaviour in this population, and present potential interventions to reduce the burden and non-compliance rates.

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林奇综合征的结肠镜检查监测是繁重的,并且经常延迟。
林奇综合征患者结直肠癌癌症风险增加,因此建议每两年进行一次结肠镜检查。我们旨在调查患者对监控的感知和偏好,并进一步探索依从性行为。林奇综合征患者接受了一项经过验证的调查,评估他们最近三次结肠镜检查的经验。如果结肠镜检查间隔不同,则个体不符合监测要求 ≥ 建议间隔6个月。291名受邀者中,共有197人(68%)返回了调查。他们大多每两年接受一次结肠镜检查(99%),在轻度镇静状态下(79%),并通过Moviprep®进行肠道准备(99%)。21%的人认为监测会影响生活质量,57%的人认为是中等到极度繁重的,尤其是40岁以下的人。为了减轻负担,患者优先考虑肠道准备的量和味道的改善、与松弛有关的排便、等待时间,以及内镜工作人员更个人化和尊重他人的方法。此外,许多人(60%)倾向于采用侵入性较小的监测方式,如生物标志物。总的来说,28%的患者延迟了结肠镜检查监测,主要是因为与患者相关的原因。另有10%的人考虑放弃/推迟监测。根据多变量分析,患者相关的延迟与低和中等教育程度、 ≤ 4次结肠镜检查,没有医院召回系统。林奇综合征的结肠镜检查监测通常是繁重的,并且经常延迟。我们确定了这一人群监测行为的决定因素,并提出了减少负担和不遵守率的潜在干预措施。
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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
期刊最新文献
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